硒
细胞内
谷胱甘肽
化学
细胞毒性
毒性
抗氧化剂
体外
细胞凋亡
谷胱甘肽过氧化物酶
生物物理学
生物化学
有机化学
酶
生物
作者
Laura Pérez-Garrido,Mariano Ortega‐Muñoz,Fernando Hernández-Matéo,Javier López-Jaramillo,Francisco Santoyo‐González
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-03-16
卷期号:16 (5): 7784-7791
被引量:5
标识
DOI:10.1007/s12274-023-5442-3
摘要
Abstract Selenium (Se) has been defined as the “Janus element”, with one face showing antioxidant activity and the other pro-oxidant activity. The biological effect of Se depends on both dose and speciation. Se nanoparticles are attracting major interest, although their large-scale preparation for biomedical applications is not trivial. We hypothesize that acid anhydride-coated carbon dots (AA-CD) are an attractive platform for preparing nanoparticles containing chemically defined Se. The reaction of AA-CD with 3-selenocyanatopropan-1-amine yields carbon dots bearing selenocyanate and carboxylate groups (CD-SeCN) that allow for tuning the hydrosolubility. CD-SeCN has a Se content of 0.36 µmol per mg of nanoparticles, and they show the typical photoluminescence of carbon dots. The selenocyanate groups (SeCN) exhibited glutathione peroxidase-like activity and cytotoxicity. Data show that antioxidant behavior differs between normal and tumor cells, and the evaluation on HEK293 and A549 cells reveals that the toxicity of CD-SeCN depends on dose, time, and intracellular glutathione (GSH) content. The toxicity of CD-SeCN decreases with the time of incubation and the cell death mechanism switches from necrosis to apoptosis, indicating that CD-SeCN is neutralized. Additionally, high levels of intracellular GSH exert a protective effect. These results support a pharmacological potential in cancers with low levels of intracellular GSH. The use of AA-CD as nanoplatforms is a general strategy that paves the way for the engineering of advanced nanosystems.
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